Top Tech Jobs & Startup Jobs

The Senior Director of Marketing Communications will build and lead communications strategies for Prolaio, aiming to enhance awareness, support growth, and ensure clear messaging across all channels. Responsibilities include managing media relations, internal communications, and collaboration with cross-functional teams.

The Associate Director will manage clinical programs by coordinating timelines and deliverables, facilitating communication across teams, and optimizing operational processes.

Lead portfolio strategy and decision frameworks for clinical and preclinical assets, drive eNPV/NPV analyses, coordinate portfolio planning, manage budgeting with Finance, run decision forums, prepare executive/Board materials, and build/manage the portfolio strategy team.

The Director of Analytical Development will lead analytical development for small molecules/oligonucleotides, ensuring compliance and robust deliverables for product development and regulatory submissions while collaborating with various teams and external partners.

The Senior Director, Internal Corporate Communications will lead internal communications strategy, engage employees, and ensure consistent messaging across the organization, especially during growth and change.

Lead global clinical operations end-to-end, overseeing clinical trial management and site management to deliver trials on time, on budget, and compliant with GCP/ICH. Build scalable operating models, manage CROs/vendors, drive enrollment and RBQM strategies, and develop high-performing teams across phases, including late-stage studies.

The Executive Director leads development business operations, overseeing budgets, forecasting, analytics, and clinical procurement while ensuring financial discipline and operational transparency.

The Executive Director of Global Site Management leads clinical trial operations, optimizing site management, enrollment, and strategic partnerships globally while ensuring compliance and high-quality data.

The Director oversees non-clinical regulatory strategy, safety assessments, and collaborates on drug development. Responsible for leading teams and managing CROs, budgets, and communication of results.

The Associate Director, External Manufacturing oversees CDMO relationships for API and DP production, ensuring compliance, efficiency, and alignment with corporate goals. Responsibilities include strategy implementation, performance management, and collaboration with internal teams for seamless operations.